NYEIS Version 4.3 (ICD) ICD - 10 Codes Available in NYEIS at time of version launch (9/23/2015)
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1 D82.1 Di George's syndrome E63.9 Nutritional deficiency, unspecified E70.21 Tyrosinemia E70.29 Other disorders of tyrosine metabolism E70.30 Albinism, unspecified E70.5 Disorders of tryptophan metabolism E70.8 Other disorders of aromatic amino acid metabolism E78.71 Barth syndrome E78.72 Smith Lemli Opitz syndrome F40.10 Social phobia, unspecified F43.10 Post traumatic stress disorder, unspecified F43.12 Post traumatic stress disorder, chronic F50.8 Other eating disorders F80.0 Phonological disorder F80.1 Expressive language disorder F80.2 Mixed receptive expressive language disorder F80.4 Speech and language development delay due to hearing loss F80.81 Childhood onset fluency disorder F80.89 Other developmental disorders of speech and language F81.9 Developmental disorder of scholastic skills, unspecified F82 Dyspraxia (Specific developmental disorder of motor function) F84.0 Autistic disorder F84.5 Asperger's syndrome F84.8 Other pervasive developmental disorders F84.9 Pervasive developmental disorder, unspecified F88 Other disorders of psychological development F89 Unspecified disorder of psychological development F90.0 Attention deficit hyperactivity disorder, predominantly inattentive type F90.1 Attention deficit hyperactivity disorder, predominantly hyperactive type F90.2 Attention deficit hyperactivity disorder, combined type F90.8 Attention deficit hyperactivity disorder, other type F90.9 Attention deficit hyperactivity disorder, unspecified type F93.8 Other childhood emotional disorders F93.9 Childhood emotional disorder, unspecified F94.0 Selective mutism F94.1 Reactive attachment disorder of childhood 1
2 F94.8 Other childhood disorders of social functioning F98.29 Other feeding disorders of infancy and early childhood F98.8 Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence F98.9 Unspecified behavioral and emotional disorders with onset usually occurring in childhood and adolescence G12.0 Infantile spinal muscular atrophy, type I [Werdnig Hoffman] G24.9 Dystonia, unspecified G Epileptic spasms, not intractable, with status epilepticus G Epileptic spasms, not intractable, without status epilepticus G Epileptic spasms, intractable, with status epilepticus G Epileptic spasms, intractable, without status epilepticus G71.2 Congenital myopathies G72.89 Other specified myopathies G72.9 Myopathy, unspecified G80.0 Spastic quadriplegic cerebral palsy G80.1 Spastic diplegic cerebral palsy G80.2 Spastic hemiplegic cerebral palsy G80.3 Athetoid cerebral palsy G80.4 Ataxic cerebral palsy G80.8 Other cerebral palsy G80.9 Cerebral palsy, unspecified G81.90 Hemiplegia, unspecified affecting unspecified side H Retinopathy of prematurity, stage 4, right eye H Retinopathy of prematurity, stage 4, left eye H Retinopathy of prematurity, stage 4, bilateral H Retinopathy of prematurity, stage 4, unspecified eye H Retinopathy of prematurity, stage 5, right eye H Retinopathy of prematurity, stage 5, left eye H Retinopathy of prematurity, stage 5, bilateral H Retinopathy of prematurity, stage 5, unspecified eye H Retrolental fibroplasia, unspecified eye H35.50 Unspecified hereditary retinal dystrophy H Coloboma of optic disc, right eye H Coloboma of optic disc, left eye H Coloboma of optic disc, bilateral H Coloboma of optic disc, unspecified eye H54.0 Blindness, both eyes 2
3 H54.1 Blindness, one eye, low vision other eye H54.10 Blindness, one eye, low vision other eye, unspecified eyes H54.2 Low vision, both eyes H54.3 Unqualified visual loss, both eyes H54.4 Blindness, one eye H54.5 Low vision, one eye H54.6 Unqualified visual loss, one eye H54.7 Unspecified visual loss H54.8 Legal blindness, as defined in USA H55.01 Congenital nystagmus H55.03 Visual deprivation nystagmus H90.0 Conductive hearing loss, bilateral H90.11 Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side H90.12 Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side H90.2 Conductive hearing loss, unspecified H90.3 Sensorineural hearing loss, bilateral H90.41 Sensorineural hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side H90.42 Sensorineural hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side H90.5 Unspecified sensorineural hearing loss H90.6 Mixed conductive and sensorineural hearing loss, bilateral H90.71 Mixed conductive and sensorineural hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side H90.72 Mixed conductive and sensorineural hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side H90.8 Mixed conductive and sensorineural hearing loss, unspecified H93.25 Central auditory processing disorder I63.50 Cerebral infarction due to unspecified occlusion or stenosis of unspecified cerebral artery I Other speech and language deficits following unspecified cerebrovascular disease I Apraxia following unspecified cerebrovascular disease K21.0 Gastro esophageal reflux disease with esophagitis M08.00 Unspecified juvenile rheumatoid arthritis of unspecified site M15.9 Polyosteoarthritis, unspecified 3
4 M19.90 Unspecified osteoarthritis, unspecified site M35.7 Hypermobility syndrome M43.6 Torticollis M53.82 Other specified dorsopathies, cervical region M62.3 Immobility syndrome (paraplegic) M62.81 Muscle weakness (generalized) M62.89 Other specified disorders of muscle M62.9 Disorder of muscle, unspecified P04.3 Newborn (suspected to be) affected by maternal use of alcohol P07.00 Extremely low birth weight newborn, unspecified weight P07.01 Extremely low birth weight newborn, less than 500 grams P07.02 Extremely low birth weight newborn, grams P07.03 Extremely low birth weight newborn, grams P07.10 Other low birth weight newborn, unspecified weight P07.34 Preterm newborn, gestational age 31 completed weeks P07.35 Preterm newborn, gestational age 32 completed weeks P14.0 Erb's paralysis due to birth injury P14.1 Klumpke's paralysis due to birth injury P14.3 Other brachial plexus birth injuries P52.22 Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn P52.3 Unspecified intraventricular (nontraumatic) hemorrhage of newborn P57.8 Other specified kernicterus P57.9 Kernicterus, unspecified P91.2 Neonatal cerebral leukomalacia P92.1 Regurgitation and rumination of newborn P92.2 Slow feeding of newborn P92.6 Failure to thrive in newborn P92.8 Other feeding problems of newborn P92.9 Feeding problem of newborn, unspecified Q01.0 Frontal encephalocele Q01.1 Nasofrontal encephalocele Q01.2 Occipital encephalocele Q01.8 Encephalocele of other sites Q01.9 Encephalocele, unspecified Q02 Microcephaly Q03.0 Malformations of aqueduct of Sylvius Q03.1 Atresia of foramina of Magendie and Luschka 4
5 Q03.8 Other congenital hydrocephalus Q03.9 Congenital hydrocephalus, unspecified Q04.0 Agenesis of corpus callosum Q04.1 Arhinencephaly Q04.2 Holoprosencephaly Q04.3 Other reduction deformities of brain Q04.5 Megalencephaly Q04.6 Congenital cerebral cysts Q04.8 Other specified congenital malformations of brain Q05.0 Cervical spina bifida with hydrocephalus Q05.1 Thoracic spina bifida with hydrocephalus Q05.2 Lumbar spina bifida with hydrocephalus Q05.3 Sacral spina bifida with hydrocephalus Q05.4 Unspecified spina bifida with hydrocephalus Q05.5 Cervical spina bifida without hydrocephalus Q05.6 Thoracic spina bifida without hydrocephalus Q05.7 Lumbar spina bifida without hydrocephalus Q05.8 Sacral spina bifida without hydrocephalus Q05.9 Spina bifida, unspecified Q07.01 Arnold Chiari syndrome with spina bifida Q07.02 Arnold Chiari syndrome with hydrocephalus Q07.03 Arnold Chiari syndrome with spina bifida and hydrocephalus Q13.1 Absence of iris Q14.2 Congenital malformation of optic disc Q16.0 Congenital absence of (ear) auricle Q16.1 Congenital absence, atresia and stricture of auditory canal (external) Q16.3 Congenital malformation of ear ossicles Q16.4 Other congenital malformations of middle ear Q16.5 Congenital malformation of inner ear Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified Q35.1 Cleft hard palate Q35.3 Cleft soft palate Q35.5 Cleft hard palate with cleft soft palate Q35.7 Cleft uvula Q35.9 Cleft palate, unspecified Q36.0 Cleft lip, bilateral 5
6 Q36.1 Cleft lip, median Q36.9 Cleft lip, unilateral Q37.0 Cleft hard palate with bilateral cleft lip Q37.1 Cleft hard palate with unilateral cleft lip Q37.2 Cleft soft palate with bilateral cleft lip Q37.3 Cleft soft palate with unilateral cleft lip Q37.4 Cleft hard and soft palate with bilateral cleft lip Q37.5 Cleft hard and soft palate with unilateral cleft lip Q37.8 Unspecified cleft palate with bilateral cleft lip Q37.9 Unspecified cleft palate with unilateral cleft lip Q45.9 Congenital malformation of digestive system, unspecified Q66.89 Other specified congenital deformities of feet Q68.0 Congenital deformity of sternocleidomastoid muscle Q68.8 Other specified congenital musculoskeletal deformities Q71.61 Lobster claw right hand Q71.62 Lobster claw left hand Q71.63 Lobster claw hand, bilateral Q Other reduction defects of unspecified upper limb Q71.90 Unspecified reduction defect of unspecified upper limb Q Other reduction defects of unspecified lower limb Q73.0 Congenital absence of unspecified limb(s) Q73.1 Phocomelia, unspecified limb(s) Q73.8 Other reduction defects of unspecified limb(s) Q74.3 Arthrogryposis multiplex congenital Q74.8 Other specified congenital malformations of limb(s) Q75.0 Craniosynostosis Q75.2 Hypertelorism Q75.9 Congenital malformation of skull and face bones, unspecified Q85.00 Neurofibromatosis, unspecified Q86.0 Fetal alcohol syndrome (dysmorphic) Q87.1 Congenital malformation syndromes predominantly associated with short stature Q87.2 Congenital malformation syndromes predominantly involving limbs Q87.3 Congenital malformation syndromes involving early overgrowth Q87.5 Other congenital malformation syndromes with other skeletal changes Q87.81 Alport syndrome 6
7 Q87.89 Other specified congenital malformation syndromes, not elsewhere classified 7 Q89.7 Multiple congenital malformations, not elsewhere classified Q89.8 Other specified congenital malformations Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction) Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction) Q90.2 Trisomy 21, translocation Q90.9 Down syndrome, unspecified Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction) Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction) Q91.2 Trisomy 18, translocation Q91.3 Trisomy 18, unspecified Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction) Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction) Q91.6 Trisomy 13, translocation Q91.7 Trisomy 13, unspecified Q99.2 Fragile X chromosome Q99.9 Chromosomal abnormality, unspecified R26.0 Ataxic gait R26.1 Paralytic gait R26.2 Difficulty in walking, not elsewhere classified R26.89 Other abnormalities of gait and mobility R26.9 Unspecified abnormalities of gait and mobility R27.0 Ataxia, unspecified R27.8 Other lack of coordination R27.9 Unspecified lack of coordination R Other symptoms and signs involving the nervous system R Other symptoms and signs involving the musculoskeletal system R29.90 Unspecified symptoms and signs involving the nervous system R29.91 Unspecified symptoms and signs involving the musculoskeletal system R47.02 Dysphasia R47.81 Slurred speech R47.89 Other speech disturbances R48.1 Agnosia R48.2 Apraxia R48.8 Other symbolic dysfunctions R62.0 Delayed milestone in childhood
8 R62.50 Unspecified lack of expected normal physiological development in childhood R62.51 Failure to thrive (child) R63.3 Feeding difficulties R69 Illness, unspecified R99 Ill defined and unknown cause of mortality S14.109A Unspecified injury at unspecified level of cervical spinal cord, initial encounter S24.109A S34.109A Unspecified injury at unspecified level of thoracic spinal cord, initial encounter Unspecified injury to unspecified level of lumbar spinal cord, initial encounter S34.139A Unspecified injury to sacral spinal cord, initial encounter Z00.8 Encounter for other general examination Z04.9 Encounter for examination and observation for unspecified reason Z13.4 Encounter for screening for certain developmental disorders in childhood 8
CONV. TYPE Unspecified pervasive developmental disorder YES NO Approx. F84.9 Pervasive developmental disorder, unspecified YES YES 307.
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